The CF Community Blog is written by the community, for the community. It's about sharing our experiences, reflections, and perspectives — the good days, the bad days, and all the tough and wonderful things in between. With topics ranging from emotional health to treatments, the blog is a platform to share your unique story.
Having an atypical presentation of CF means I stand somewhere between the CF world and the rest of the world — and that makes me feel like I belong in neither.
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Meet a few faces from the 2015 Pittsburgh's 50 Finest event and learn how they raised funds and awareness for the CF cause.
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Learn why Anna Kampas, a young adult with CF, faces her challenging treatment regimen head on.
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I have found my existence as a cystic fibrosis adolescent to be very interesting. This is mostly because in addition to the acne and braces and intense hormonal imbalances, there was always my CF.
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I read the blogs and stories parents write about their compliant CF kids, I hear CF adults speak about never missing a treatment or medication, and despite my best efforts, I am fighting a battle I never imagined with Betsy.
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Before you can walk a mile in a person with CF's shoes, you have to put on a nebulizer.
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Learn how one college junior went from struggling with CF at school to managing it with flying colors.